Project Manager, Oncology - Sponsor Dedicated

Accountabilities:

• • Lead interdisciplinary oncology clinical research projects, overseeing study execution from launch through conduct and closeout.
  • Serve as the primary liaison between the organization and the sponsor, ensuring studies are delivered according to contractual commitments, timelines, quality standards, and expectations.
  • Lead project teams and coordinate study partners to maintain quality, timelines, budget performance, and overall delivery.
  • Monitor project financial performance, proactively identify issues, and implement appropriate corrective and risk-mitigation strategies.
  • Ensure study activities comply with Good Clinical Practice (GCP), applicable SOPs, ICH guidelines, and relevant regulatory requirements.
  • Maintain accountability for project deliverables, study documentation, and the quality and completeness of the Trial Master File (TMF).
  • Maintain accurate study information across relevant databases and systems.
  • Support inspection readiness by overseeing study management activities, documentation, project plans, and compliance processes.
  • Plan, coordinate, and lead internal and external meetings, while preparing clear project reports for sponsors and leadership.
  • Develop contingency plans and risk mitigation strategies to address potential delivery challenges.
  • Build strong sponsor relationships and identify opportunities for future or expanded collaboration.
  • Participate in proposal or bid-defense activities when selected as a potential project manager.
  • Provide leadership or line management support to project management and clinical monitoring team members when required.

  Requirements:

  • Bachelor’s degree or equivalent qualification in life sciences, medicine, pharmacy, nursing, or a related discipline; equivalent combinations of education and experience may also be considered.
  • Relevant experience within a clinical research organization (CRO) and direct oncology or other therapeutic-area experience is preferred.
  • Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable clinical research regulations.
  • Demonstrated experience managing clinical research projects, including timelines, budgets, deliverables, risks, and cross-functional teams.
  • Strong organizational and time-management skills, with the ability to manage multiple priorities independently.
  • Excellent written and verbal communication, presentation, and interpersonal skills.
  • Strong leadership and stakeholder-management capabilities, with the ability to build effective sponsor and project-team relationships.
  • Ability to analyze project risks, develop contingency plans, and proactively resolve issues.
  • Comfortable adopting new technologies and working in technology-enabled clinical research environments.
  • Ability and willingness to travel as required, approximately 25%.

  Benefits:

  • Fully remote work opportunity within the United States.
  • Medical, dental, and vision healthcare benefits.
  • 401(k) program with company matching.
  • Employee Stock Purchase Plan eligibility.
  • Potential eligibility for company- and individual-performance bonuses or commissions.
  • Flexible paid time off (PTO) and sick time, subject to applicable local requirements.
  • Potential company car or car allowance, depending on role and eligibility.
  • Career development and progression opportunities.
  • Therapeutic-area and technical training, peer recognition, and professional development support.
  • Opportunity to collaborate with global clinical research and biopharmaceutical experts.
  • Exposure to emerging technologies, data, scientific resources, and complex clinical development programs.